Medical DevicesNationwide
Beckman Coulter Inc ACCESS Estradiol Reagent Test System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ACCESS Estradiol Reagent Test System
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Lot number 215173
Products Sold
Lot number 215173
Beckman Coulter Inc is recalling ACCESS Estradiol Reagent Test System due to Short volume, resulting possibility of falsely elevated results.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Short volume, resulting possibility of falsely elevated results.
Recommended Action
Per FDA guidance
Consignees were notified by letter dated may 8, 2003. It requests destruction of inventory for credit.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026